Veterinary compositions of modified virus-like particles of cmv and il-1 beta mutein antigens

Abstract

The present invention relates to compositions comprising modified virus-like particles (VLPs) of Cucumber Mosaic Virus (CMV), and in particular to modified VLPs of CMV comprising chimeric CMV polypeptides which comprise a stretch of consecutive negative amino acids selected from aspartic acid and/or glutamic acid to which specific Interleukin-1β mutein antigens, IL-1β-D145X antigens, are linked, as well as pharmaceutical compositions thereof, which compositions preferably serve as vaccines for generating immune responses, in particular antibody responses, against IL-1β.

1 . A composition, optionally a veterinary composition, comprising
 (a) a modified VLP of CMV, wherein said modified VLP of CMV comprises at least one first attachment site, and wherein said modified VLP of CMV comprises at least one chimeric CMV polypeptide, wherein said at least one chimeric CMV polypeptide comprises, a CMV polypeptide, wherein said CMV polypeptide comprises a coat protein of CMV or an amino acid sequence having a sequence identity of at least 75% with SEQ ID NO:45; and   (b) at least one antigen, wherein said antigen comprises at least one second attachment site, and wherein said antigen is an interleukin 1β D145X mutein (IL-1 β-D145X mutein) antigen; and   
       wherein (a) and (b) are linked through said at least one first and said at least one second attachment site, optionally via at least one covalent non-peptide bond. 
     
     
         2 . A composition, optionally a veterinary composition, comprising
 (a) a modified VLP of CMV, wherein said modified VLP of CMV comprises at least one first attachment site, and wherein said modified VLP of CMV comprises at least one chimeric CMV polypeptide, wherein said at least one chimeric CMV polypeptide comprises,
 (i) a CMV polypeptide, wherein said CMV polypeptide comprises a coat protein of CMV or an amino acid sequence having a sequence identity of at least 75% with SEQ ID NO:45; and 
 (ii) a polypeptide comprising a stretch of consecutive negative amino acids, wherein said negative amino acids are independently selected from aspartic acid and/or glutamic acid, wherein said polypeptide is inserted between any amino acid residue of said CMV polypeptide corresponding to any amino acid residue between position 75 and position 85 of SEQ ID NO:45. 
   (b) at least one antigen, wherein said antigen comprises at least one second attachment site, and wherein said antigen is an interleukin 1β D145X mutein (IL-1 β-D145X mutein) antigen; and   wherein (a) and (b) are linked through said at least one first and said at least one second attachment site, optionally via at least one covalent non-peptide bond.   
     
     
         3 . The composition of  claim 1 , wherein said chimeric CMV polypeptide further comprises a T helper cell epitope, wherein said T helper cell epitope replaces a N-terminal region of said CMV polypeptide, wherein said N-terminal region of said CMV polypeptide corresponds to amino acids 2-12 of SEQ ID NO:45. 
     
     
         4 . The composition of  claim 3 , wherein said T helper cell epitope comprises the amino acid sequence of SEQ ID NO:47 or SEQ ID NO:48. 
     
     
         5 . The composition of CMV of  claim 1 , wherein said CMV polypeptide is a coat protein of CMV or an amino acid sequence having a sequence identity of at least 90%, optionally 95% with SEQ ID NO:45. 
     
     
         6 . The composition of  claim 2 , wherein said CMV polypeptide comprises the amino acid sequence of SEQ ID NO:5, wherein said polypeptide comprising said stretch of consecutive negative amino acids is inserted between amino acid residues of position 88 and position 89 of said SEQ ID NO:5. 
     
     
         7 . The composition of CMV of  claim 2 , wherein said stretch of consecutive negative amino acids has a length of 3 to 10 amino acids. 
     
     
         8 . The composition of CMV of  claim 2 , wherein said stretch of consecutive negative amino acids consists solely of glutamic acids. 
     
     
         9 . The composition of CMV of  claim 2 , wherein said polypeptide comprising said stretch of consecutive negative amino acids further comprises a first amino acid linker and a second amino acid linker, wherein said first amino acid linker is positioned at the N-terminus of said stretch of consecutive negative amino acids, and said second amino acid linker is positioned at the C-terminus of said stretch of consecutive negative amino acids, and wherein said first and said second amino acid linker is independently selected from the group consisting of:
 (a.) a polyglycine linker (G-linker) having an amino acid sequence (Gly) n of a length of n=2-10;   (b.) a glycine-serine linker (GS-linker) comprising at least one glycine and at least one serine, wherein optionally said GS linker has an amino acid sequence of (GS) r (G s S) t (GS) u  with r=0 or 1, s=1-5, t=1-5 and u=0 or 1; and   (c.) an amino acid linker (GS*-linker) comprising at least one Gly, at least one Ser, and at least one amino acid selected from Thr, Ala, Lys, and Cys.   
     
     
         10 . The composition of  claim 1 , wherein said polypeptide comprises SEQ ID NO: 49, SEQ ID NO:50 or SEQ ID NO:51. 
     
     
         11 . The composition of  claim 1 , wherein said chimeric CMV polypeptide comprises the amino acid sequence of SEQ ID NO:10, SEQ ID NO:11 or SEQ ID NO:12. 
     
     
         12 . The composition of  claim 2 , wherein said at least one first attachment site is not comprised or part of the polypeptide comprising said stretch of consecutive negative amino acid. 
     
     
         13 . The composition of  claim 1 , wherein said first attachment site is an amino group, optionally an amino group of a lysine residue, and wherein said at least one second attachment site is a sulfhydryl group, optionally a sulfhydryl group of a cysteine residue. 
     
     
         14 . The composition of  claim 1 , wherein said antigen is selected from an interleukin 1β D145K mutein (IL-1β-D145K mutein) antigen. 
     
     
         15 . A method of inducing neutralizing antibodies against IL-1β in an animal wherein said method comprising administering a composition of  claim 1 . 
     
     
         16 . (canceled) 
     
     
         17 . The composition of  claim 2 , wherein said chimeric CMV polypeptide further comprises a T helper cell epitope, wherein said T helper cell epitope replaces a N-terminal region of said CMV polypeptide, wherein said N-terminal region of said CMV polypeptide corresponds to amino acids 2-12 of SEQ ID NO:45. 
     
     
         18 . The composition of  claim 17 , wherein optionally said T helper cell epitope comprises the amino acid sequence of SEQ ID NO:47 or SEQ ID NO:48. 
     
     
         19 . The composition of CMV of  claim 2 , wherein said CMV polypeptide is a coat protein of CMV or an amino acid sequence having a sequence identity of at least 90%, optionally 95% with SEQ ID NO:45. 
     
     
         20 . The composition of CMV of  claim 2 , wherein said CMV polypeptide comprises the amino acid sequence of SEQ ID NO:5, wherein said polypeptide comprising said stretch of consecutive negative amino acids is inserted between amino acid residues of position 88 and position 89 of said SEQ ID NO:5. 
     
     
         21 . The composition of  claim 2 , wherein said chimeric CMV polypeptide comprises the amino acid sequence of SEQ ID NO:10, SEQ ID NO:11 or SEQ ID NO:12.